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NM_000059.4(BRCA2):c.8663G>C (p.Arg2888Pro) AND Breast-ovarian cancer, familial, susceptibility to, 2

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jul 10, 1998
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV000113982.2

Allele description [Variation Report for NM_000059.4(BRCA2):c.8663G>C (p.Arg2888Pro)]

NM_000059.4(BRCA2):c.8663G>C (p.Arg2888Pro)

Gene:
BRCA2:BRCA2 DNA repair associated [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
13q13.1
Genomic location:
Preferred name:
NM_000059.4(BRCA2):c.8663G>C (p.Arg2888Pro)
HGVS:
  • NC_000013.11:g.32376700G>C
  • NG_012772.3:g.66221G>C
  • NM_000059.4:c.8663G>CMANE SELECT
  • NP_000050.2:p.Arg2888Pro
  • NP_000050.3:p.Arg2888Pro
  • LRG_293t1:c.8663G>C
  • LRG_293:g.66221G>C
  • LRG_293p1:p.Arg2888Pro
  • NC_000013.10:g.32950837G>C
  • NM_000059.3:c.8663G>C
  • U43746.1:n.8891G>C
Protein change:
R2888P
Links:
dbSNP: rs80359124
NCBI 1000 Genomes Browser:
rs80359124
Molecular consequence:
  • NM_000059.4:c.8663G>C - missense variant - [Sequence Ontology: SO:0001583]
Observations:
1

Condition(s)

Name:
Breast-ovarian cancer, familial, susceptibility to, 2 (BROVCA2)
Synonyms:
Breast-ovarian cancer, familial 2
Identifiers:
MONDO: MONDO:0012933; MedGen: C2675520; Orphanet: 145; OMIM: 612555

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000147432Breast Cancer Information Core (BIC) (BRCA2)
no assertion criteria provided
Uncertain significance
(Jul 10, 1998) 		germlineclinical testing

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyes1not providednot providednot providednot providedclinical testing

Details of each submission

From Breast Cancer Information Core (BIC) (BRCA2), SCV000147432.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot provided1not providednot providednot provided

Last Updated: Sep 29, 2024